Submission Details

Submitter:

Classification:
Strong
GENCC:100002
Gene:
Disease:
congenital primary aphakia
OMIM:610256
Mode Of Inheritance:
Autosomal recessive
Evaluated Date:
05/31/2021
PubMed IDs:
10652278 16199865 16826526 17064680 19708017 20140963 20361012 25504734 26995144 27218149 27669367 28418495 29136273 29314435
Assertion Criteria:
Submitter Submitted Date:
11/30/2023

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